Informaţii despre

Nume Fragile X Syndrome
Pagina Web www.malacards.org
Clasificare globală Malacards Boli fetale; Boli genetice; Boli rare
Clasificari ICD10 Fragile X chromosome
Clasificare anatomică Malacards Boli ale ochiului; Boli ale sistemului reproducator; Boli endocrine; Boli neuronale; Boli psihice
Boli din aceeaşi familie Fragile X Syndrome Type 1; Fragile X Syndrome Type 2; Fragile X Syndrome Type 3

Vezi şi

Boli A-Z 46,xy Gonadal Dysgenesis, Partial, with Minifascicular Neuropathy Achondroplasia Adie Pupil Aging Alacrima, Achalasia, and Mental Retardation Syndrome Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity Alport Syndrome, X-Linked Al-Raqad Syndrome Androgen Insensitivity Syndrome, Mild Angelman Syndrome Aniridia 1 Anorexia Nervosa 1 Arthrochalasia Ehlers-Danlos Syndrome Ataxia and Polyneuropathy, Adult-Onset Atrial Septal Defect 1 Attention Deficit-Hyperactivity Disorder Audiogenic Seizures Autism Autism Spectrum Disorder Autism X-Linked 2 Autoimmune Disease Benign Childhood Occipital Epilepsy, Panayiotopoulos Type Blood Group--Ahonen Blood Group, Dombrock System Blood Group, I System Body Mass Index Quantitative Trait Locus 10 Body Mass Index Quantitative Trait Locus 11 Body Mass Index Quantitative Trait Locus 12 Body Mass Index Quantitative Trait Locus 14 Body Mass Index Quantitative Trait Locus 18 Body Mass Index Quantitative Trait Locus 4 Body Mass Index Quantitative Trait Locus 7 Body Mass Index Quantitative Trait Locus 8 Body Mass Index Quantitative Trait Locus 9 Central Nervous System Disease Cerebellar Atrophy, Developmental Delay, and Seizures Cerebritis Cherubism Chorea, Childhood-Onset, with Psychomotor Retardation Choreatic Disease Cluttering Cognitive Function 1, Social Collecting Duct Carcinoma Congenital Nystagmus Costello Syndrome Cutis Verticis Gyrata Cystic Fibrosis Diabetes Insipidus Disease of Mental Health Down Syndrome Dysostosis Dysphasia, Familial Developmental Epilepsy Fanconi Anemia, Complementation Group E Fetal Alcohol Syndrome Fmr1-Related Primary Ovarian Insufficiency Focal Epilepsy Fragile X-Associated Tremor/ataxia Syndrome Fragile X Tremor/ataxia Syndrome Global Developmental Delay, Absent or Hypoplastic Corpus Callosum, and Dysmorphic Facies Hepatic Adenomas, Familial Hepatitis Hereditary Spastic Paraplegia Ichthyosis Ichthyosis Prematurity Syndrome Infertility Kagami-Ogata Syndrome Kaposiform Hemangioendothelioma Kaufman Oculocerebrofacial Syndrome Learning Disability Lutheran Suppressor, X-Linked Mbd25-Related Intellectual Disability Mbd5 Haploinsufficiency Medulloblastoma Mental Retardation, X-Linked, Associated with Fragile Site Fraxe Monosomy 21 Muscular Atrophy Muscular Dystrophy Mutism Myoclonic Epilepsy of Lafora Myoclonus Myoclonus Epilepsy Myotonic Dystrophy Neurodegeneration with Brain Iron Accumulation 2a Neurofibromatosis, Type Iv, of Riccardi Neuronitis Otitis Media Paraplegia Pervasive Developmental Disorder Phelan-Mcdermid Syndrome Piebald Trait Prader-Willi Syndrome Precocious Puberty Premature Menopause Progressive Myoclonus Epilepsy Pyogenic Sterile Arthritis, Pyoderma Gangrenosum, and Acne Rett Syndrome Smith-Magenis Syndrome Spasticity Specific Developmental Disorder Specific Language Impairment Spinal Muscular Atrophy Status Epilepticus Striatal Degeneration, Autosomal Dominant 2 Stuttering Testicular Microlithiasis Tic Disorder Transmitted_by Tremor Tuberous Sclerosis Turner Syndrome Velocardiofacial Syndrome Werner Syndrome Williams-Beuren Syndrome X-Linked Disease